Compare the 3 manufacturers holding an active US Drug Master File for Goserelin API, with DMF numbers and filing years from the FDA's quarterly DMF list.
Directory listing last reviewed October 2026.
3 manufacturers hold an active Type II Drug Master File for GoserelinAPI, taken from the FDA's quarterly DMF list; 2 of them are listed in this directory. A DMF lets a drug applicant reference the maker's manufacturing data. It is not an FDA approval. Check each manufacturer against the FDA import alert lists before ordering.
| Manufacturer | Location | US DMF | Filed |
|---|---|---|---|
| ALP Pharm Beijing | China (Beijing) | 29713 | 2015 |
| Bachem Holding AG | Switzerland / USA | 34363, 35689 | 2019 |
Not yet listed in this directory, so we have not reviewed them. Names as printed in the FDA DMF list.
| DMF holder | US DMF | Filed |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | 31488 | 2017 |
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